Abstract
The role of human choroid plexus (CP) epithelium in the transport of solutes between the blood and the cerebrospinal fluid and/or in secretion processes may be studied by employing several experimental approaches. There are a number of in vitro techniques for human CP epithelium (CPE) and all have limitations that do not exclude them a priori, but that should be carefully taken into consideration. Developmental and morphological studies have been largely performed on human choroid plexus samples of either embryonic or post-mortem origin. Functional uptake studies may be performed on pathologically unaltered CP samples obtained during surgical removal of choroid plexus tumors. This approach can be used to explore transport processes mainly across the apical side of the CPE, but cannot be used to study vectorial transport across the CPE. Also, these samples have limited viability. A monolayer of CPE in culture, grown on permeable supports, provides the best available tool to study transport processes or polarized secretion by the CP, but thus far only limited attempts to culture these cells have been published and they mainly include data from neoplastic CPE. A study that used a human papilloma-derived cell line in culture showed that it forms a monolayer with barrier properties, although the cells express pleomorphic and neoplastic features and lack contact inhibition. Other cell cultures express some CPE markers but do not develop tight junctions/barrier properties. This article reviews the main characteristics and limitations of available in vitro methods to study human CPE, which could help researchers choose an appropriate experimental approach for a particular study.
Highlights
A constant and well-controlled composition of extracellular fluid in the central nervous system (CNS) is essential for neuronal processing
A careful interpretation of acquired data is essential for achieving the correct conclusions, since it is clear that findings obtained from these cell cultures cannot be directly extrapolated to the in vivo situation
Other available choroid plexus (CP) cultures could be used to explore processes that do not require the presentation of barrier function
Summary
A constant and well-controlled composition of extracellular fluid in the central nervous system (CNS) is essential for neuronal processing. Abbreviations ABCB1: ATP-binding cassette sub-family B member 1, known as Pglycoprotein; ABCB4: ATP-binding cassette, sub-family B, member 4, known as MDR3; ABCC1: Multidrug resistance-associated protein 1; BCSFB: Blood-cerebrospinal fluid barriers; CP: Choroid plexus; CPC: CP carcinoma; CPE: CP epithelium; CRL: Crown-rump length; CSF: Cerebrospinal fluid; DMEM: Dulbecco’s Modified Eagle Medium; ECF: Extracellular fluid; FCS: Fetal calf serum; HBSS: Hank’s Buffered Salt Solution; hCNTs: Human concentrative nucleoside transporters; hENTs: Human equilibrative nucleoside transporters; HIBCPP: Human malignant choroid plexus papilloma cell line; TEER: Transendothelial electrical resistance; TJ: Tight junctions
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